Genetics University — Research, Education, Medical Genetics
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Gene entry

IL7R

interleukin 7 receptor

Chromosome
5
Cytoband
5p13.2
Variants (rsID)
16

IL7R is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p13.2). Its official name is “interleukin 7 receptor”. The reference table lists 16 variants (rsID) for this gene.

Clinically classified variants

15 reference-table entries with clinical significance.

  • rs10063294Benignsingle nucleotide variantImmunodeficiency 104
  • rs1494555Benignsingle nucleotide variantImmunodeficiency 104
  • rs1494558Benignsingle nucleotide variantImmunodeficiency 104
  • rs3194051Benignsingle nucleotide variantImmunodeficiency 104
  • rs41270321Benignsingle nucleotide variantImmunodeficiency 104
  • rs6897932Benignsingle nucleotide variantImmunodeficiency 104
  • rs193922642Conflicting interpretationssingle nucleotide variantSevere combined immunodeficiency disease|Immunodeficiency 104
  • rs193922640Likely pathogenicDuplicationSevere combined immunodeficiency disease
  • rs193922645Likely pathogenicsingle nucleotide variantSevere combined immunodeficiency disease
  • rs104893894Pathogenicsingle nucleotide variantImmunodeficiency 104
  • rs193922641Pathogenicsingle nucleotide variantSevere combined immunodeficiency disease|Immunodeficiency 104
  • rs587778405Pathogenicsingle nucleotide variantImmunodeficiency 104
  • rs141919625Uncertain significancesingle nucleotide variantImmunodeficiency 104
  • rs148001159Uncertain significancesingle nucleotide variantImmunodeficiency 104
  • rs193922647Uncertain significancesingle nucleotide variant

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.